Evidence map›Paper›PMID 25712213›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2015

Macrophage migration inhibitory factor-CXCR4 is the dominant chemotactic axis in human mesenchymal stem cell recruitment to tumors.

Sofia Lourenco, Vitor H Teixeira, Tammy Kalber, Ricardo J Jose, R Andres Floto, Sam M Janes

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed
6.1field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

88 citing papers in PubMed, 155 citations in OpenAlex.

  1. Article
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  6. Review
  7. Mesenchymal Stem Cells in Cancer Therapy.Advances in experimental medicine and biology · 2025
    Review
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  9. Article
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  15. Article
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  18. Article
  19. Review
  20. TGFβJournal of cellular and molecular medicine · 2023
    Article

28 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 3 countries.

Sofia LourencoLungs for Living Research Centre, Division of Medicine, University College London, London WC1E 6JF, United Kingdom; s.janes@ucl.ac.uk.
Vitor H TeixeiraLungs for Living Research Centre, Division of Medicine, University College London, London WC1E 6JF, United Kingdom;
Tammy KalberLungs for Living Research Centre, Division of Medicine, University College London, London WC1E 6JF, United Kingdom; University College London Centre of Advanced Biomedical Imaging, University College London, London WC1E 6DD, United Kingdom;
Ricardo J JoseCentre for Inflammation and Tissue Repair, Division of Medicine, University College London, London WC1E 6JF, United Kingdom; and.
R Andres FlotoCambridge Institute for Medical Research, Department of Medicine, University of Cambridge, Cambridge, CB2 0XY, United Kingdom.
Sam M JanesLungs for Living Research Centre, Division of Medicine, University College London, London WC1E 6JF, United Kingdom;
University College London · GBCambridge School · PTCentre for Inflammation Research · GBLiving Streets · GB

Funding

Cancer Research UKDepartment of HealthMedical Research Council MR/M015831/1Wellcome Trust 091730Wellcome Trust 097216/z/11/zWellcome Trust 100140Wellcome Trust WT091730MA
6 · The paper itself

Abstract

Mesenchymal stromal cells (MSCs) are inherently tumor homing and can be isolated, expanded, and transduced, making them viable candidates for cell therapy. This tumor tropism has been used to deliver anticancer therapies to various tumor models. In this study, we sought to discover which molecules are the key effectors of human MSC tumor homing in vitro and using an in vivo murine model. In this study, we discover a novel role for macrophage migration inhibitory factor (MIF) as the key director of MSC migration and infiltration toward tumor cells. We have shown this major role for MIF using in vitro migration and invasion assays, in presence of different receptor inhibitors and achieving a drastic decrease in both processes using MIF inhibitor. Additionally, we demonstrate physical interaction between MIF and three receptors: CXCR2, CXCR4, and CD74. CXCR4 is the dominant receptor used by MIF in the homing tumor context, although some signaling is observed through CXCR2. We demonstrate downstream activation of the MAPK pathway necessary for tumor homing. Importantly, we show that knockdown of either CXCR4 or MIF abrogates MSC homing to tumors in an in vivo pulmonary metastasis model, confirming the in vitro two-dimensional and three-dimensional assays. This improved understanding of MSC tumor tropism will further enable development of novel cellular therapies for cancers.

Indexed as

Antigens, Differentiation, B-LymphocyteBreast NeoplasmsCell Line, TumorChemotaxisCulture Media, ConditionedGene Expression ProfilingGene Knockdown TechniquesHistocompatibility Antigens Class IIHumansLung NeoplasmsMacrophage Migration-Inhibitory FactorsMAP Kinase Kinase 1MAP Kinase Kinase 2Mesenchymal Stem CellsNeoplasmsProtein BindingAntigens, Differentiation, B-LymphocyteCulture Media, ConditionedHistocompatibility Antigens Class IIinvariant chainMacrophage Migration-Inhibitory FactorsMAP Kinase Kinase 1MAP Kinase Kinase 2Proto-Oncogene Proteins c-rafReceptors, CXCR4Receptors, Interleukin-8B

Identifiers

PMID25712213
PMCPMC4374168
OpenAlexW2127755727

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.